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Metabolic SyndromePrevMetSynNCT01959763

Prevention of the Metabolic Syndrome by New Lifestyle Intervention Methods

A study testing Weight loss counseling program in people with Metabolic Syndrome and Obesity, run by University of Oulu at 1 site in Finland.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This intervention aims to reduce obesity by using new type of nutritional and lifestyle therapy and in parallel, tailored persuasive information and communications technology (ICT)-technology based application. The study hypothesis is that obesity cannot be reduced just by distributing nutritional information. Read more about this study

Who is it for?
Ages 20 to 60 years
Conditions the study is for
Metabolic Syndrome, Obesity, Overweight
What is being tested?
Weight loss counseling program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
574 participants
Where
1 siteFinland
Study dates
Feb 2013to Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • BMI 27-35

Who cannot join

  • Other concurrent weight loss programs
  • Disease which prevents weight loss
  • Medication which affects on weight loss

Trial locations and contacts

1 site in 1 country.

Finland1 site
  • Oulu University Hospital

    Oulu, 90220

Other trials in Finland

About this study

Official title: Prevention of the Metabolic Syndrome by a Lifestyle Intervention - an Application of the New Intervention Methods in the Primary Health Care.

This intervention aims to reduce obesity by using new type of nutritional and lifestyle therapy and in parallel, tailored persuasive information and communications technology (ICT)-technology based application. The study hypothesis is that obesity cannot be reduced just by distributing nutritional information. Instead, by influencing also the eating behavior, permanent lifestyle changes can be achieved. The effect of the therapy along the time-line, the health information literacy of the study persons and the changes in it will be studied at different phases of the intervention. The research will be carried out in three main groups of different levels of nutritional therapies with a parallel ICT-intervention and control group for each main group (altogether six groups).

Read the detailed description

The research objectives of this study: 1) to find the best counseling methods for improving eating behavior (group counseling, tailored web-based counseling), 2) to find the predictors of successful lifestyle changes and weight loss, 3) to find the associations with biological and psychological eating behavior regulation system, 4) to study the long-term effects of the intervention, 5) to investigate the changes to the medications after the intervention . The study hypothesis is that new theoretically valid cognitive-behavioral-therapy -based counseling methods in combination with ICT support based on persuasive design improve eating behavior, weight loss and self-efficacy and reduce risk factors for the metabolic syndrome, type 2 diabetes, coronary heart disease and musculoskeletal factors.

The study population consists of participants with overweight or obesity and at least one risk factor of metabolic syndrome (MetSyn). A population-based sample of 600 participants living in the Oulu area (approx. 200 000 habitants) is collected with the help of the Finnish Population Register Centre.

Inclusion criteria include also the ability to use basic ICT technology (email etc.). Exclusion criteria are certain uncontrolled health factors, such as abnormal laboratory values (thyroid, kidney and liver function tests) or clinically significant illness with contraindication for weight loss or physical activity.

Study visits are at baseline, 1, 2 and 5 years. At the study visit blood samples are drawn at the research laboratory of the Oulu University Hospital. Along with the timeline of the visits the eating behaviour factors (emotional eating, uncontrolled eating and cognitive restraint), health information literacy (HIL), nutrition habits, smoking, alcohol consumption, medication and previous diseases are recorded by a detailed questionnaires sent to study persons by e-mail. The blood pressure, waist diameter, height and weight are also measured during the visit. All the operations have been described in detail and accepted by the regional Ethics Committee of the Northern Ostrobothnia.

The randomization process is two-phased. First the subjects who are included in the study are randomized into 2 different kinds of lifestyle face-to-face counselling groups and one control group. After that they are randomized into users or non-users of the web-based ICT-program "Onnikka". As a summary, there are six different counselling groups: 1) Intensive group counselling, 2) Intensive group counselling with Onnikka, 3) Short term group counselling, 4) Short term counselling with Onnikka, 5) Control group (no intervention at all), and 6) Only Onnikka.

A linear mixed-effect model (LMM) (as primary analysis), where group (six study arms) and time were fixed effect factors are used to examine the differences in weight from baseline to 1, 2 and 5 years adjusting for age and sex. Primary analysis and sensitivity analyses are based on intention-to-treat principles. Primary analysis are also used to examine the differences between ICT groups and non-ICT groups. Group and time interaction are included in the model to examine whether mean change over time is different between groups. If data include missing values, they will be assumed to be completely at random. The same model is used with imputed values (both last observation carried forward (LOCF) and return-to-baseline (RTB) where data are missing and for completers as sensitivity analyses. Area Under the Curve (AUC) analysis is performed to integrate the effect interventions on the weight reduction over the different time points.

Being tested
Weight loss counseling program
Keywords
Metabolic syndrome, obesity, overweight, weight loss intervention, cognitive behavioral therapy, ICT intervention, cardiovascular disease, persuasive systems design
Medical subject headings
Metabolic Syndrome, Obesity, Overweight, Cardiovascular Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Weight loss counseling programBehavioural

    Also called PrevMetSyn, Prevent Metabolic Syndrome

    Randomized study persons are given either one of the two different methods of weight loss counseling program without ICT or with ICT-based counseling. As a control for the study groups one group is receiving only ICT-based counseling and one group does not receive any of the counseling methods.

Study groups in NCT01959763
Study groupRoleWhat they receive
Weight loss counseling with ICT interventionExperimentalCognitive behavioral therapy-based weight loss counseling program including 8 group visits. Participant have also persuasive ICT support.
Receives: Behavioral: Weight loss counseling program
Weigth loss counselingExperimentalCognitive behavioral therapy-based weight loss counseling program including 8 group visits.
Receives: Behavioral: Weight loss counseling program
ELVIRA-based weight loss counseling with ICT interventionExperimentalWeight loss counseling program based on 2 group visits of ELVIRA counseling method. Participant have also persuasive ICT support.
Receives: Behavioral: Weight loss counseling program
ELVIRA-based weight loss counselingExperimentalWeight loss counseling program based on 2 group visits of ELVIRA counseling method.
Receives: Behavioral: Weight loss counseling program
ICT-based weight loss counselingExperimentalICT-based weight loss counseling program with 52 weekly tasks and information packages.
Receives: Behavioral: Weight loss counseling program
Control groupExperimentalUsual care without any interventions.
Receives: Behavioral: Weight loss counseling program

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Weight change

    Measured: Baseline, 1 , 2 and 5 years

Secondary outcomes (1)
  1. Change in eating behavior

    emotional eating, uncontrolled eating, cognitive restraint, binge eating symptoms

    Measured: Baseline, 1, 2 and 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted10 Oct 2013 (estimated)
  2. Study startFeb 2013
  3. Primary completionDec 2019
  4. Study completionDec 2025 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Factorial
Masking
None (open label)
Enrolment
574 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01959763
Sponsor's protocol ID
55/2012
Other IDs
083/THL/TE/2012
Acronym
PrevMetSyn
Status last verified
Oct 2024
First submitted
6 Sep 2013
Last updated
31 Oct 2024
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Publications

  • Rahunen R, Merikallio H, Rinne V, Savolainen MJ, Hukkanen J. Hypertension in Overweight and Obesity: Sex-Specific Role of 4beta-Hydroxycholesterol. J Am Heart Assoc. 2026 Mar 3;15(5):e043913. doi: 10.1161/JAHA.125.043913. Epub 2026 Feb 26.

    PubMed 41744113
  • Turkkila E, Pekkala T, Merikallio H, Merikukka M, Heikkila L, Hukkanen J, Oinas-Kukkonen H, Salonurmi T, Teeriniemi AM, Jokelainen T, Savolainen MJ. Five-year follow-up of a randomized weight loss trial on a digital health behaviour change support system. Int J Obes (Lond). 2025 May;49(5):949-953. doi: 10.1038/s41366-025-01742-4. Epub 2025 Mar 15.

    PubMed 40089569

Questions about this trial

What is this clinical trial studying?

A study testing Weight loss counseling program in people with Metabolic Syndrome and Obesity, run by University of Oulu at 1 site in Finland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 31 Oct 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Finland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Weight change (time frame: Baseline, 1 , 2 and 5 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01959763, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 31 Oct 2024.

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